Pettmann B, Manthorpe M, Powell J A, Varon S
Department of Biology, University of California San Diego, La Jolla 92093.
J Neurosci. 1988 Oct;8(10):3624-32. doi: 10.1523/JNEUROSCI.08-10-03624.1988.
We have previously developed a cell-blot technique to visualize directly in tissue extracts molecules that display the biological activity of ciliary neuronotrophic factors (CNTFs). This technique involves SDS-PAGE of the tissue extract, Western blotting on nitrocellulose paper, neuronal cell culture on the paper, and, using a vital dye, visualization of the neurons that selectively survive on the trophic factor band. In this report, we show that (1) NGF, either purified or in a crude extract from submaxillary glands, can also be successfully recognized using a slightly modified cell-blot technique; (2) a variety of ganglionic neurons can respond to distinct nitrocellulose-anchored trophic factors; (3) while CNTF and NGF can both support the survival of their common target cells, only NGF also promotes neuritic extension; and (4) both the dimeric and the monomeric forms of immobilized beta-NGF are active.
我们之前开发了一种细胞印迹技术,可在组织提取物中直接可视化显示睫状神经营养因子(CNTF)生物活性的分子。该技术包括对组织提取物进行SDS-PAGE、在硝酸纤维素纸上进行蛋白质印迹、在纸上进行神经元细胞培养,以及使用活性染料对在营养因子条带上选择性存活的神经元进行可视化。在本报告中,我们表明:(1)使用略有改进的细胞印迹技术,纯化的或来自颌下腺粗提物中的NGF也能被成功识别;(2)多种神经节神经元可对不同的固定在硝酸纤维素上的营养因子作出反应;(3)虽然CNTF和NGF都能支持其共同靶细胞的存活,但只有NGF还能促进神经突延伸;(4)固定化的β-NGF的二聚体和单体形式均具有活性。